IECG

GUDID 00884838093478

Philips Medical Systems

Medical equipment clinical data interfacing software

• Primary Device ID: 00884838093478
• NIH Device Record Key: ba25afb9-a9df-4be4-b0d4-5b0754e2f327
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IECG
• Version Model Number: B.02
• Company DUNS: 078628040
• Company Name: Philips Medical Systems
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

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Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838093478 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120855

FDA Product Code

• DQK: Computer, diagnostic, programmable

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-10-22
• Device Publish Date: 2019-10-14

On-Brand Devices [IECG]

• 00884838090750: B.01
• 00884838032408: B.01.00
• 00884838093478: B.02